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rs7692181

From SNPedia

Orientationplus
Stabilizedplus
Make rs7692181(C;C)
Make rs7692181(C;T)
Make rs7692181(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position63635276
is asnp
is mentioned by
dbSNPrs7692181
ebirs7692181
HLIrs7692181
Exacrs7692181
Varsomers7692181
Maprs7692181
PheGenIrs7692181
hapmaprs7692181
1000 genomesrs7692181
hgdprs7692181
ensemblrs7692181
gopubmedrs7692181
geneviewrs7692181
scholarrs7692181
googlers7692181
pharmgkbrs7692181
gwascentralrs7692181
openSNPrs7692181
23andMers7692181
23andMe allrs7692181
SNP Nexus

SNPshotrs7692181
SNPdbers7692181
MSV3drs7692181
GWAS Ctlgrs7692181
GMAF0.2815
Max Magnitude
? (C;C) (C;T) (T;T) 28


GET Evidence
rs7692181
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.296875
summary